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DO Term : Fanconi anemia complementation group T [DOID:0111081] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32.

synonyms:
FANCT,
616435,
OMIM:616435

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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